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8. Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS. Valoti E; Alberti M; Iatropoulos P; Piras R; Mele C; Breno M; Cremaschi A; Bresin E; Donadelli R; Alizzi S; Amoroso A; Benigni A; Remuzzi G; Noris M Front Immunol; 2019; 10():853. PubMed ID: 31118930 [TBL] [Abstract][Full Text] [Related]
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11. Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome. Hofer J; Janecke AR; Zimmerhackl LB; Riedl M; Rosales A; Giner T; Cortina G; Haindl CJ; Petzelberger B; Pawlik M; Jeller V; Vester U; Gadner B; van Husen M; Moritz ML; Würzner R; Jungraithmayr T; Clin J Am Soc Nephrol; 2013 Mar; 8(3):407-15. PubMed ID: 23243267 [TBL] [Abstract][Full Text] [Related]
12. Clinical and Genetic Characteristics of Atypical Hemolytic Uremic Syndrome in Children: A Chinese Cohort Study. Wu D; Chen J; Ling C; Chen Z; Fan J; Sun Q; Meng Q; Liu X Nephron; 2021; 145(4):415-427. PubMed ID: 33873197 [TBL] [Abstract][Full Text] [Related]
13. [Analysis of variants in complement genes in Han Chinese children with atypical hemolytic uremic syndrome]. Yi CL; Zhao F; Qiu HZ; Wang LM; Huang J; Nie XJ; Yu ZH Zhonghua Er Ke Za Zhi; 2017 Aug; 55(8):624-627. PubMed ID: 28822440 [No Abstract] [Full Text] [Related]
14. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome. Zipfel PF; Edey M; Heinen S; Józsi M; Richter H; Misselwitz J; Hoppe B; Routledge D; Strain L; Hughes AE; Goodship JA; Licht C; Goodship TH; Skerka C PLoS Genet; 2007 Mar; 3(3):e41. PubMed ID: 17367211 [TBL] [Abstract][Full Text] [Related]
15. Variants in complement genes are uncommon in patients with anti-factor H autoantibody-associated atypical hemolytic uremic syndrome. Khandelwal P; Joshi A; Mathur A; Puraswani M; Gurjar BS; Sinha A; Hari P; Faruq M; Bagga A Pediatr Nephrol; 2023 Aug; 38(8):2659-2668. PubMed ID: 36622444 [TBL] [Abstract][Full Text] [Related]
16. Factor D Inhibition Blocks Complement Activation Induced by Mutant Factor B Associated With Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis. Aradottir SS; Kristoffersson AC; Roumenina LT; Bjerre A; Kashioulis P; Palsson R; Karpman D Front Immunol; 2021; 12():690821. PubMed ID: 34177949 [TBL] [Abstract][Full Text] [Related]
17. Favorable four-yr outcome after renal transplantation in a patient with complement factor H antibody and CFHR1/CFHR3 gene mutation-associated HUS. Grenda R; Jarmużek W; Rubik J; Prokurat S; Miklaszewska M; Drozdz D; Zachwieja K; Ardissino G; Hofer J Pediatr Transplant; 2015 Sep; 19(6):E130-4. PubMed ID: 26087050 [TBL] [Abstract][Full Text] [Related]
18. Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. Osborne AJ; Breno M; Borsa NG; Bu F; Frémeaux-Bacchi V; Gale DP; van den Heuvel LP; Kavanagh D; Noris M; Pinto S; Rallapalli PM; Remuzzi G; Rodríguez de Cordoba S; Ruiz A; Smith RJH; Vieira-Martins P; Volokhina E; Wilson V; Goodship THJ; Perkins SJ J Immunol; 2018 Apr; 200(7):2464-2478. PubMed ID: 29500241 [TBL] [Abstract][Full Text] [Related]
19. A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome. Francis NJ; McNicholas B; Awan A; Waldron M; Reddan D; Sadlier D; Kavanagh D; Strain L; Marchbank KJ; Harris CL; Goodship TH Blood; 2012 Jan; 119(2):591-601. PubMed ID: 22058112 [TBL] [Abstract][Full Text] [Related]
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